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| Content Provider | Springer Nature Link |
|---|---|
| Author | Bosco, Nazario Lange, Titia |
| Copyright Year | 2012 |
| Abstract | Mouse telomeres have been suggested to resemble common fragile sites (CFS), showing disrupted TTAGGG fluorescent in situ hybridization signals after aphidicolin treatment. This “fragile” telomere phenotype is induced by deletion of TRF1, a shelterin protein that binds telomeric DNA and promotes efficient replication of the telomeric ds[TTAGGG]n tracts. Here we show that the chromosome-internal TTAGGG repeats present at human chromosome 2q14 form an aphidicolin-induced CFS. TRF1 binds to and stabilizes CFS 2q14 but does not affect other CFS, establishing 2q14 as the first CFS controlled by a sequence-specific DNA binding protein. The data show that telomeric DNA is inherently fragile regardless of its genomic position and imply that CFS can be caused by a specific DNA sequence. |
| Starting Page | 465 |
| Ending Page | 474 |
| Page Count | 10 |
| File Format | |
| ISSN | 00095915 |
| Journal | Chromosoma |
| Volume Number | 121 |
| Issue Number | 5 |
| e-ISSN | 14320886 |
| Language | English |
| Publisher | Springer-Verlag |
| Publisher Date | 2012-07-13 |
| Publisher Place | Berlin, Heidelberg |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Eukaryotic Microbiology Animal Genetics and Genomics Human Genetics Cell Biology Biochemistry Developmental Biology |
| Content Type | Text |
| Resource Type | Article |
| Subject | Genetics Genetics (clinical) |
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